For researchers
Is your paper here?
2,663 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
7 matches for
Cole JB.
Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes
Huerta-Chagoya A,
Schroeder P,
Mandla R,
Li J,
Morris L,
Vora M,
Alkanaq A,
Nagy D,
Szczerbinski L,
Madsen JGS,
Bonàs-Guarch S,
Mollandin F
and 14 more — show all
Cole JB,
Porneala B,
Westerman K,
Li JH,
Pollin TI,
Florez JC,
Gloyn AL,
Carey DJ,
Cebola I,
Mirshahi UL,
Manning AK,
Leong A,
Udler M,
Mercader JM
Nature genetics · 2024 · PMID 39379762 · open access
12 pages+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
and 73 more — show all
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
and 76 more — show all
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
The impact of non-additive genetic associations on age-related complex diseases
Guindo-Martínez M,
Amela R,
Bonàs-Guarch S,
Puiggròs M,
Salvoro C,
Miguel-Escalada I,
Carey CE,
Cole JB,
Rüeger S,
Atkinson E,
Leong A,
Sanchez F
and 9 more — show all
FinnGen Consortium
Nature communications · 2021 · PMID 33893285 · open access
5 pages
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo
Jin Y,
Birlea SA,
Fain PR,
Ferrara TM,
Ben S,
Riccardi SL,
Cole JB,
Gowan K,
Holland PJ,
Bennett DC,
Luiten RM,
Wolkerstorfer A
and 19 more — show all
van der Veen JP,
Hartmann A,
Eichner S,
Schuler G,
van Geel N,
Lambert J,
Kemp EH,
Gawkrodger DJ,
Weetman AP,
Taïeb A,
Jouary T,
Ezzedine K,
Wallace MR,
McCormack WT,
Picardo M,
Leone G,
Overbeck A,
Silverberg NB,
Spritz RA
Nature genetics · 2012 · PMID 22561518 · open access
3 pages
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
Sandholm N,
Cole JB,
Nair V,
Sheng X,
Liu H,
Ahlqvist E,
van Zuydam N,
Dahlström EH,
Fermin D,
Smyth LJ,
Salem RM,
Forsblom C
and 19 more — show all
Valo E,
Harjutsalo V,
Brennan EP,
McKay GJ,
Andrews D,
Doyle R,
Looker HC,
Nelson RG,
Palmer C,
McKnight AJ,
Godson C,
Maxwell AP,
Groop L,
McCarthy MI,
Kretzler M,
Susztak K,
Hirschhorn JN,
Florez JC,
Groop PH
GENIE Consortium
Diabetologia · 2022 · PMID 35763030 · open access
2 pages
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.